Summary
The FDA issued a Class II for item 8201810 FLUFF BAR 78x2.75 OZ, NET WT 12.07 LB by FGF, LLC. Reason: potential for contamination with listeria monocytogenes.
Details
Source
Food Recall
External ID
F-0478-2025
Action Date
2025-02-12
Status
Terminated
Category
food
Product Description
item 8201810 FLUFF BAR 78x2.75 OZ, NET WT 12.07 LB
Lot/Code Info: All product within expiration produced 12/13/24 and prior
Quantity Affected: 2,017,614 cases total
Reason for Recall
potential for contamination with listeria monocytogenes
Distribution
Nationwide US and Canada
Type: Voluntary: Firm initiated
Recall Initiated: 2025-01-07
Company
Brownsburg, IN
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 106 food recalls issued in the same week, part of 204 food-related FDA actions this month.
FGF, LLC has 60 FDA actions in our database, including 60 recalls.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (FGF, LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does FGF, LLC have FDA actions?
FGF, LLC has 60 FDA actions in our database, including 60 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0478-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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